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Keramatipour, Mohammad
89  results:
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1

Distinct neurological phenotypes associated with biallelic ..:

Tasharrofi, Behnoosh ; Najafi, Ali ; Pourbakhtyaran, Elham...
Molecular Biology Reports.  51 (2024)  1 - p. , 2024
Link: https://doi.org/10.1007/..
 
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2

A novel missense variant in EIF2B5 identified in a consangu..:

Nourmohammadi, Parisa ; Asadollahi, Mostafa ; Karamzade, Arezou...
Journal of Genetics.  102 (2023)  2 - p. , 2023
Link: https://doi.org/10.1007/..
 
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3

A rare immunological disease, caspase 8 deficiency: case re..:

Bazgir, Narges ; Tahvildari, Azin ; Chavoshzade, Zahra...
Allergy, Asthma & Clinical Immunology.  19 (2023)  1 - p. , 2023
Link: https://doi.org/10.1186/..
 
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4

Clinical, Immunological, and Genetic Findings in Iranian Pa..:

Mousavi Khorshidi, Mohadese Sadat ; Seeleuthner, Yoann ; Chavoshzadeh, Zahra...
Journal of Clinical Immunology.  43 (2023)  8 - p. 1941-1952 , 2023
Link: https://doi.org/10.1007/..
 
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5

Author Correction: Integrated genomic sequencing in myeloid..:

Kazemi‑Sefat, Golnaz Ensieh ; Keramatipour, Mohammad ; Vaezi, Mohammad...
Scientific Reports.  13 (2023)  1 - p. , 2023
Link: https://doi.org/10.1038/..
 
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6

Intestinal hypomagnesemia in an Iranian patient with a nove..:

Kamali, Farnaz ; Jamee, Mahnaz ; Sayer, John A....
CEN Case Reports.  12 (2023)  4 - p. 413-418 , 2023
Link: https://doi.org/10.1007/..
 
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7

Integrated genomic sequencing in myeloid blast crisis chron..:

Kazemi-Sefat, Golnaz Ensieh ; Keramatipour, Mohammad ; Vaezi, Mohammad...
Scientific Reports.  12 (2022)  1 - p. , 2022
Link: https://doi.org/10.1038/..
 
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8

Novel PGM3 mutation in two siblings with combined immunodef..:

Fallahi, Mazdak ; Jamee, Mahnaz ; Enayat, Javad...
Allergy, Asthma & Clinical Immunology.  18 (2022)  1 - p. , 2022
Link: https://doi.org/10.1186/..
 
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9

Waardenburg syndrome type 2A in a large Iranian family with..:

Zardadi, Safoura ; Rayat, Sima ; Hassani Doabsari, Maryam..
BMC Medical Genomics.  14 (2021)  1 - p. , 2021
Link: https://doi.org/10.1186/..
 
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10

Four mutations in MITF, SOX10 and PAX3 genes were identifie..:

Zardadi, Safoura ; Rayat, Sima ; Doabsari, Maryam Hassani...
BMC Pediatrics.  21 (2021)  1 - p. , 2021
Link: https://doi.org/10.1186/..
 
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11

SPOAN syndrome: a novel mutation and new ocular findings; a..:

Bazvand, Fatemeh ; Keramatipour, Mohammad ; Riazi-Esfahani, Hamid.
BMC Neurology.  21 (2021)  1 - p. , 2021
Link: https://doi.org/10.1186/..
 
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12

The importance of CDC27 in cancer: molecular pathology and ..:

Kazemi-Sefat, Golnaz Ensieh ; Keramatipour, Mohammad ; Talebi, Saeed...
Cancer Cell International.  21 (2021)  1 - p. , 2021
Link: https://doi.org/10.1186/..
 
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13

X-linked SCID with a rare mutation:

Mahdavi, Fatemeh Sadat ; Keramatipour, Mohammad ; Ansari, Sarina...
Allergy, Asthma & Clinical Immunology.  17 (2021)  1 - p. , 2021
Link: https://doi.org/10.1186/..
 
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14

Identification of a novel truncating variant in AHI1 gene a..:

Karamzade, Arezou ; Babaei, Meisam ; Saberi, Mohammad...
Molecular Biology Reports.  48 (2021)  6 - p. 5339-5345 , 2021
Link: https://doi.org/10.1007/..
 
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15

Exome sequencing reveals novel rare variants in Iranian fam..:

Salehi, Zahra ; Keramatipour, Mohammad ; Talebi, Saeed...
Genomics.  113 (2021)  4 - p. 2645-2655 , 2021
Link: https://doi.org/10.1016/..
 
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